HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925572Generated: October 26, 2026
9-oxo-9H-pyrrolo[1,2-a]indole-5-carboxylic acid (4-aminopyridin-3-yl)amide → HCID 67072884, compound
https://huagongshe.com/reaction/1925572
Participants
| Role | Name | HCID | Charge |
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| Reactant | 9-oxo-9H-pyrrolo[1,2-a]indole-5-carboxylic acid (4-aminopyridin-3-yl)amide | HCID 67299358 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 67072884 | HCID 67072884 | 46.1% |
Reaction Steps
In a 20 ml microwave reactor, a mixture of 256 mg of 9-oxo-9H-pyrrolo[1,2-a]indole-5-carboxylic acid (4-aminopyridin-3-yl)amide obtained according to the preceding stage, in 20 ml of glacial acetic acid, is heated at 200° C. for 30 minutes. The reaction medium is filtered through clarcel, washing being carried out with glacial acetic acid. The filtrate is evaporated to dryness under vacuum and the residue is taken up twice with toluene and each time re-evaporated to dryness under vacuum. The solid is triturated from isopropyl ether, filtered, and dried under vacuum at 40° C. overnight. 111 mg of 5-(3H-imidazo[4,5-c]pyridin-2-yl)pyrrolo[1,2-a]indol-9-one are obtained in the form of a solid, the characteristics of which are the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178687B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-cd8eeddff9144481bd321ffc907f4d29 |
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| Source note | uspto-grants-2012_05 |
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